United States · FDA National Drug Code directory
Ondansetron Hydrochloride
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 51655-933_4960f7bf-1a44-0802-e063-6394a90a2855
- Product NDC
- 51655-933
- Form
- TABLET, FILM COATED
- Composition / generic term
- Ondansetron Hydrochloride
- Labeler
- Northwind Health Company, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220720
- Source listing expiry
- 20271231
Source-listed ingredients
- ONDANSETRON HYDROCHLORIDE — 4 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 4 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-933-04) · 51655-933-04
- 3 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-933-43) · 51655-933-43
- 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-933-53) · 51655-933-53
- 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-933-54) · 51655-933-54
- 5 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-933-55) · 51655-933-55
- 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-933-87) · 51655-933-87
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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